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一种基于新型荧光绿色荧光蛋白发色团类似物的定量PCR染料。

A Novel Fluorescent GFP Chromophore Analog-Based Dye for Quantitative PCR.

作者信息

Stakheev A A, Ryazantsev D Yu, Zvezdina Yu K, Baranov M S, Zavriev S K

机构信息

Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow, 117997, Russia.

出版信息

Biochemistry (Mosc). 2018 Jul;83(7):855-860. doi: 10.1134/S000629791807009X.

DOI:10.1134/S000629791807009X
PMID:30200870
Abstract

This is the first report describing the possibility of using a green fluorescent protein chromophore synthetic analog, P-HOBDI-BF, as a fluorescent dye for a linear hydrolysis probe used in qPCR. The study was carried out on a system for detection of the plant pathogenic fungus Fusarium avenaceum using a plasmid containing translation elongation factor 1α fragment as a template. To estimate fluorogenic properties of P-HOBDI-BF, 6-FAM- and BDP-FL-labeled probes were used. It was demonstrated that a synthetic dye based on the P-HOBDI-BF chromophore can be used for labeling hydrolysis probes for qPCR, but fluorescence increase levels for P-HOBDI-BF-labeled probes were slightly lower than those for 6-FAM-labeled ones. At the same time, the sensitivity of P-HOBDI-BF-based assays remained high, and this fact together with acceptable fluorescence levels suggests that this dye can be considered as an efficient alternative for reporters traditionally used for fluorescence detection in the FAM channel.

摘要

这是首篇描述使用绿色荧光蛋白发色团合成类似物P-HOBDI-BF作为实时定量聚合酶链反应(qPCR)中线性水解探针荧光染料可能性的报告。该研究以一个检测植物病原真菌燕麦镰刀菌的系统进行,使用含有翻译延伸因子1α片段的质粒作为模板。为评估P-HOBDI-BF的荧光特性,使用了6-羧基荧光素(6-FAM)和BDP-FL标记的探针。结果表明,基于P-HOBDI-BF发色团的合成染料可用于标记qPCR的水解探针,但P-HOBDI-BF标记探针的荧光增加水平略低于6-FAM标记的探针。同时,基于P-HOBDI-BF的检测灵敏度仍然很高,这一事实与可接受的荧光水平表明,这种染料可被视为传统上用于FAM通道荧光检测的报告分子有效替代品。

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